Canonical Allele Identifier: CA1250829316
Gene:

Linked Data

dbSNP Id: rs1668654702

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722344A>C , CM000664.2:g.52722344A>C GRCh38
NC_000002.11:g.52949482A>C , CM000664.1:g.52949482A>C GRCh37
NC_000002.10:g.52802986A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.913T>G